Canonical Allele Identifier: CA360812274

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755595T>G (hg19) ; chr5:g.132419903T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419903T>G , CM000667.2:g.132419903T>G	GRCh38
NC_000005.9:g.131755595T>G , CM000667.1:g.131755595T>G	GRCh37
NC_000005.8:g.131783494T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-246T>G	ENSP00000492349.2:n.-246T>G
ENST00000638504.1:n.169T>G
ENST00000638568.2:c.-388T>G	ENSP00000491158.2:n.-388T>G
ENST00000639899.1:n.212T>G
ENST00000337752.6:c.11T>G (CARINH)	ENSP00000338228.2:p.Leu4Arg
ENST00000378947.7:c.11T>G (CARINH)	ENSP00000368230.3:p.Leu4Arg
ENST00000378953.8:c.11T>G (CARINH)	ENSP00000368236.4:p.Leu4Arg
ENST00000407797.5:c.11T>G (CARINH)	ENSP00000385513.1:p.Leu4Arg
ENST00000461203.5:n.142T>G (CARINH)
ENST00000621237.1:c.11T>G (CARINH)	ENSP00000481774.1:p.Leu4Arg
NR_045116.1:n.350T>G (CARINH)
NM_001207001.2:c.11T>G (CARINH)	NP_001193930.1:p.Leu4Arg
XR_948788.3:n.894-154A>C (LINC02863)
NR_161242.1:n.194T>G (CARINH)